Evidence map›Paper›PMID 25644422›Full record

ArticleNeuroscience2015

Thalamic adenylyl cyclase 1 is required for barrel formation in the somatosensory cortex.

A Suzuki, L-J Lee, Y Hayashi, L Muglia, S Itohara, R S Erzurumlu, T Iwasato

Open access · bronzeAbstract read
In one paragraph

Article in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Adenylyl Cyclases as Therapeutic Targets in Neuroregeneration.International journal of molecular sciences · 2025
    Review
  2. Review
  3. Article
  4. CaFrontiers in pharmacology · 2022
    Review
  5. Retinal Axon Interplay for Binocular Mapping.Frontiers in neural circuits · 2021
    Article
  6. How the Barrel Cortex Became a Working Model for Developmental Plasticity: A Historical Perspective.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  7. Review
  8. Development of tactile sensory circuits in the CNS.Current opinion in neurobiology · 2018
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Glutamate input in the dorsal raphe nucleus as a determinant of escalated aggression in male mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 3 countries.

A SuzukiDivision of Neurogenetics, National Institute of Genetics (NIG), Mishima, Shizuoka 411-8540, Japan; Department of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka 411-8540, Japan.
L-J LeeDepartment of Anatomy and Cell Biology, National Taiwan University, Taipei, Taiwan.
Y HayashiLaboratory for Behavioral Genetics, RIKEN Brain Science (BSI) Institute, Wako, Saitama 351-0198, Japan.
L MugliaPerinatal Institute, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
S ItoharaLaboratory for Behavioral Genetics, RIKEN Brain Science (BSI) Institute, Wako, Saitama 351-0198, Japan.
R S ErzurumluDepartment of Anatomy and Neurobiology, University of Maryland, Baltimore, MD 21201-1075, USA.
T IwasatoDivision of Neurogenetics, National Institute of Genetics (NIG), Mishima, Shizuoka 411-8540, Japan; Department of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka 411-8540, Japan. Electronic address: tiwasato@nig.ac.jp.
National Institute of Genetics · JPRIKEN Center for Brain Science · JPNational Taiwan University · TWUniversity of Cincinnati · USUniversity of Maryland, Baltimore · US

Funding

SOMATOSENSORY CORTICAL DEVELOPMENT AND PLASTICITYR01NS039050 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 2000 to 2013
$4.6M
Consequences of Developmental Defects in Somatosensory Map formationR01NS084818 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 2014 to 2024
$4.2M
CELLULAR MECHANISMS UNDERLYING PATTERN FORMATIONR01NS037070 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 1998 to 2013
$3.4M
Thalamocortical circuit defects in developmental brain disordersR01NS092216 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 2015 to 2019
$2.9M
NINDS NIH HHS R01 NS037070NINDS NIH HHS R01 NS039050NINDS NIH HHS R01 NS084818NINDS NIH HHS R01 NS092216
6 · The paper itself

Abstract

Cyclic AMP signaling is critical for activity-dependent refinement of neuronal circuits. Global disruption of adenylyl cyclase 1 (AC1), the major calcium/calmodulin-stimulated adenylyl cyclase in the brain, impairs formation of whisker-related discrete neural modules (the barrels) in cortical layer 4 in mice. Since AC1 is expressed both in the thalamus and the neocortex, the question of whether pre- or postsynaptic (or both) AC1 plays a role in barrel formation has emerged. Previously, we generated cortex-specific AC1 knockout (Cx-AC1KO) mice and found that these animals develop histologically normal barrels, suggesting a potentially more prominent role for thalamic AC1 in barrel formation. To determine this, we generated three new lines of mice: one in which AC1 is disrupted in nearly half of the thalamic ventrobasal nucleus cells in addition to the cortical excitatory neurons (Cx/pTh-AC1KO mouse), and another in which AC1 is disrupted in the thalamus but not in the cortex or brainstem nuclei of the somatosensory system (Th-AC1KO mouse). Cx/pTh-AC1KO mice show severe deficits in barrel formation. Th-AC1KO mice show even more severe disruption in barrel patterning. In these two lines, single thalamocortical (TC) axon labeling revealed a larger lateral extent of TC axons in layer 4 compared to controls. In the third line, all calcium-stimulated adenylyl cyclases (both AC1 and AC8) are deleted in cortical excitatory neurons. These mice have normal barrels. Taken together, these results indicate that thalamic AC1 plays a major role in patterning and refinement of the mouse TC circuitry.

Indexed as

Adenylyl CyclasesAnimalsAxonsImmunohistochemistryMice, KnockoutNeuroanatomical Tract-Tracing TechniquesNeuronal PlasticitySomatosensory CortexThalamusVibrissaeadenylyl cyclase 1Adenylyl Cyclasesconditional knockoutCre/loxP systemmouseneuronal circuitrefinementsomatosensory system

Identifiers

PMID25644422
PMCPMC5994750
OpenAlexW2062133636

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.